Baroni Sara, Carletti Tea, Donalisio Manuela, Arduino Irene, Cazzaniga Irene, Giorgino Toni, Esposito Francesca, Porta Alessia, Diomede Luisa, De Luigi Ada, Gobbi Marco, Lembo David, Marcello Alessandro, Tramontano Enzo, Milani Mario, Mastrangelo Eloise
Department of Molecular Biochemistry and Pharmacology, Istituto di Ricerche Farmacologiche Mario Negri Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milano, Italy.
Laboratory of Molecular Virology, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Front Cell Infect Microbiol. 2024 Nov 25;14:1487604. doi: 10.3389/fcimb.2024.1487604. eCollection 2024.
Coronaviruses (CoVs) share key genomic elements critical for viral replication, suggesting the feasibility of developing therapeutics with efficacy across different viruses. In a previous work, we demonstrated the antiviral activity of the antipsychotic drug lurasidone against both SARS-CoV-2 and HCoV-OC43. In this study, our investigations on the mechanism of action of lurasidone suggested that the drug exhibits antiviral activity by targeting the papain-like protease (PL-Pro) of both viruses, and the Spike protein of SARS-CoV-2, thereby hampering both the entry and the viral replication. assays demonstrate that lurasidone significantly reduces viral load in infected cells, showing that the drug is a promising candidate for further development as a dual-action antiviral, offering a potential new strategy in the fight against COVID-19 and other coronavirus-related diseases.
冠状病毒(CoVs)具有对病毒复制至关重要的关键基因组元件,这表明开发对不同病毒均有效的治疗方法具有可行性。在先前的一项研究中,我们证明了抗精神病药物鲁拉西酮对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)和人冠状病毒OC43(HCoV-OC43)均具有抗病毒活性。在本研究中,我们对鲁拉西酮作用机制的研究表明,该药物通过靶向这两种病毒的木瓜样蛋白酶(PL-Pro)以及SARS-CoV-2的刺突蛋白来发挥抗病毒活性,从而阻碍病毒的进入和复制。实验证明鲁拉西酮可显著降低感染细胞中的病毒载量,表明该药物作为一种双效抗病毒药物具有进一步开发的潜力,为抗击2019冠状病毒病(COVID-19)和其他冠状病毒相关疾病提供了一种潜在的新策略。